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The Continental Source of Glyoxal Estimated by the Synergistic Use of Spaceborne Measurements and Inverse Modelling

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The Continental Source of Glyoxal Estimated by the Synergistic Use of Spaceborne Measurements and Inverse Modelling Atmos. Chem. Phys., 9, 8431–8446, 2009 www.atmos-chem-phys.net/9/8431/2009/ Atmospheric © Author(s) 2009. This work is distributed under Chemistry the Creative Commons Attribution 3.0 License. and Physics The continental source of glyoxal estimated by the synergistic use of spaceborne measurements and inverse modelling T. Stavrakou1, J.-F. Muller¨ 1, I. De Smedt1, M. Van Roozendael1, M. Kanakidou2, M. Vrekoussis3, F. Wittrock3, A. Richter3, and J. P. Burrows3,4 1Belgian Institute for Space Aeronomy, Avenue Circulaire 3, 1180, Brussels, Belgium 2ECPL, Department of Chemistry, University of Crete, Heraklion, Greece 3Institute of Environmental Physics, University of Bremen, Bremen, Germany 4Centre for Ecology and Hydrology, Maclean Building, Benson Lane, Crowmarsh Gifford, Wallingford, Oxfordshire, OX10 8BB, UK Received: 15 April 2009 – Published in Atmos. Chem. Phys. Discuss.: 19 June 2009 Revised: 21 September 2009 – Accepted: 11 October 2009 – Published: 5 November 2009 Abstract. Tropospheric glyoxal and formaldehyde columns succeeds in reducing the underestimation of the glyoxal retrieved from the SCIAMACHY satellite instrument in 2005 columns by the model, but it leads to a severe overestima- are used with the IMAGESv2 global chemistry-transport tion of glyoxal surface concentrations in comparison with in model and its adjoint in a two-compound inversion scheme situ measurements. In the second scenario, the inferred total designed to estimate the continental source of glyoxal. The global continental glyoxal source is estimated at 108 Tg/yr, formaldehyde observations provide an important constraint almost two times higher than the global a priori source. on the production of glyoxal from isoprene in the model, The extra secondary source is the largest contribution to the since the degradation of isoprene constitutes an important global glyoxal budget (50%), followed by the production source of both glyoxal and formaldehyde. Current modelling from isoprene (26%) and from anthropogenic NMVOC pre- studies underestimate largely the observed glyoxal satellite cursors (14%). A better performance is achieved in this case, columns, pointing to the existence of an additional land gly- as the updated emissions allow for a satisfactory agreement oxal source of biogenic origin. We include an extra glyoxal of the model with both satellite and in situ glyoxal observa- source in the model and we explore its possible distribu- tions. tion and magnitude through two inversion experiments. In the first case, the additional source is represented as a direct glyoxal emission, and in the second, as a secondary forma- 1 Introduction tion through the oxidation of an unspecified glyoxal precur- sor. Besides this extra source, the inversion scheme opti- Glyoxal (CHOCHO) and formaldehyde (HCHO) are short- mizes the primary glyoxal and formaldehyde emissions, as lived intermediate products in the oxidation of non-methane well as their secondary production from other identified non- volatile organic compounds (NMVOCs) emitted by vege- methane volatile organic precursors of anthropogenic, pyro- tation, fires and anthropogenic activities. They are also genic and biogenic origin. directly emitted during fossil fuel and biofuel combustion In the first inversion experiment, the additional direct and biomass burning. Both compounds absorb in the UV- source, estimated at 36 Tg/yr, represents 38% of the global visible spectral region and have been measured by the SCIA- continental source, whereas the contribution of isoprene is MACHY satellite sensor since 2003, and more recently, by equally important (30%), the remainder being accounted for the OMI and GOME-2 instruments. by anthropogenic (20%) and pyrogenic fluxes. The inversion Although current modelling studies succeed in reproduc- ing reasonably well the variability and the magnitude of the observed HCHO columns (Fu et al., 2007; Barkley et al., Correspondence to: T. Stavrakou 2008; Stavrakou et al., 2009a), a large underestimation of the ([email protected]) glyoxal columns has been reported (Myriokefalitakis et al., Published by Copernicus Publications on behalf of the European Geosciences Union. 8432 Stavrakou et al.: Estimation of the glyoxal land source 2008; Fu et al., 2008). These discrepancies point to the ex- leading to glyoxal formation after a number of non-specified istence of additional land and marine sources, and/or to an intermediate steps. These compounds could be directly emit- underestimation of the known sources. This study aims at ted or produced in the oxidation of short-lived biogenic pre- determining the global distribution and strength of the gly- cursors like terpenoids. Detailed knowledge on the oxida- oxal continental sources. To this purpose, we utilize syner- tion mechanisms and glyoxal yield of such compounds is gistically HCHO and CHOCHO satellite columns in a two- still lacking. Moreover, the release of glyoxal from organic compound inverse modelling framework based on the adjoint aerosols is another potentially significant source of glyoxal. of the IMAGES model (Muller¨ and Stavrakou, 2005). In The next section provides a description of the IMAGESv2 this approach, information gained from HCHO can help to model. Particular focus is given on the description of the constrain the sources of CHOCHO, since both gases have chemistry of the glyoxal precursors (Sect. 2.3) and to the for- common precursors and are interrelated through chemistry mation of secondary organic aerosols (Sect. 2.4) due to its (e.g. through the OH fields). Note that the focus of this study importance as a glyoxal loss process. A short description is limited to continental regions due to an inherent difficulty of the glyoxal and formaldehyde observed columns is given to retrieve CHOCHO columns over the oceans (interference in Sect. 2.5. The global glyoxal budget calculated with the with liquid water absorption (Wittrock et al., 2006)), and to model is discussed in Sect. 3. The setup for the inversion and the fact that the HCHO columns over oceanic regions lie the optimization results are presented in Sect. 4. Conclusions close to the detection limit of the instrument. are drawn in the last section. The adjoint inversion model technique is used to calcu- late the sensitivities of the discrepancy between the model and the observations with respect to a number of emis- 2 The model and the measurements sion parameters. This calculation is performed simulta- 2.1 The IMAGESv2 CTM neously for all the control variables, and thus, inversions at the horizontal resolution of the model can be afforded. The global IMAGESv2 chemistry-transport model (Muller¨ This approach, also termed as grid-based inversion, is con- and Stavrakou, 2005; Stavrakou et al., 2009a) is run at the sidered as the most efficient tool available in order to ex- horizontal resolution of 4◦×5◦ and is vertically discretized ploit the wealth of satellite measurements of reactive gases at 40 sigma-pressure levels extending from the surface to and aerosols. In particular, this method allows for address- 44 hPa. The model calculates the concentrations of 80 trace ing non-linearities and chemical interdependencies between gases using a one-day time step. Advection is driven by trace gases, for refining the spatiotemporal flux distribu- monthly mean ECMWF reanalysed wind fields, whereas tions, while distinguishing between emission types. It has daily ECMWF fields are used for temperature, water vapor, been successfully applied in the inversion of CO emissions cloud optical depths, and planetary boundary layer mixing. (Stavrakou and Muller¨ , 2006; Kopacz et a., 2009), NOx emis- Dry deposition velocities for reactive gases are calculated sions (Stavrakou et al., 2008), secondary inorganic aerosols using a resistance-in-series scheme (Wesely, 1989), whereas (Henze et al., 2009), and has been used to constrain the py- the wet scavenging parameterization is thoroughly described rogenic and biogenic NMVOC sources of HCHO based on a in the Supplement : http://www.atmos-chem-phys.net/9/ 4-year satellite dataset (Stavrakou et al., 2009b). A similar 8431/2009/acp-9-8431-2009-supplement.pdf. The model setup will be used in this study in order to derive a “top- accounts for the impact of diurnal variations of the chem- down” inventory of the glyoxal land fluxes. ical compounds through correction factors computed via a In the current inversion framework, primary formalde- diurnal cycle simulation with a 20-min time step. The di- hyde and glyoxal emission and secondary production from urnal profiles are also used to estimate the CHOCHO and NMVOC precursors (anthropogenic, biogenic and pyro- HCHO concentration at the satellite overpass time (10:00 LT) genic) are optimized for the year 2005, as well as an ad- from the daily averaged values calculated with a time step ditional missing source of glyoxal of biogenic origin. Two of one day. They depend on the location and the month. inversion experiments are investigated. In the first, the ex- The comparison with ground-based observations uses the di- tra source is assumed to be directly emitted glyoxal, and urnally averaged glyoxal concentrations. This is justified in the second, glyoxal is formed through oxidation of an since for most of the campaigns the air samples are col- unknown glyoxal precursor (UVOC) with a lifetime of five lected during 24 h and the given values are daily mean con- days. The impact of the choice for the UVOC lifetime is as- centrations. The model is confronted with the data following sessed through sensitivity
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